Does anyone know of anything other than melanin that Fontana Masson
would stain? Also, does anyone know of a stain that would label
un/saturated fatty acids? Not sure if this is even possible. Thanks in
advance.
Kris Kalleberg
___
Histonet mailing
Does anyone know of any travel positions? I have traveled in the past for a
couple of years and I have 7 years experience all together. I am willing to go
anywhere. Thanks
Leah Cox
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
Hi everyone,
I am hoping you all can help me solve a problem that I am having with
my Bcl-2 stain. I can get it to stain Follicular Lymphoma tissues, but
for the life of me can not
get normal tonsil tissue to stain. I use a Retrieval solution with a
pH of 8, use Avidin / Biotin solutions,
I haven't tried it directly but I don't see why not. If it's an amplification
problem you can always amplify the fluorescence. That being said I am really
not a huge fan of IF on FFPE especially when it comes to vessels as many
vessels have high autofluorescence not to mention the
Hi,
I have been making up my own tris buffer for immunohistochemistry. It has
been working swimmingly, with one exception. I have been doing some work on
Salmonella, and apparently the researcher has been seeing bacteria in her
immunofluorescent slides that she says are moving and seem to be
Fontana-Masson also stains for Argentaffin granuals.
Cindy Pyse, CLT, HT (ASCP)
Histology Supervisor
X-Cell Laboratories
e-mail cp...@x-celllab.com
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Any histological structure able to reduce silver into a black precipitate
(argentaffin reaction) will be stained with the Fontana-Masson procedure.
René J.
--- On Wed, 2/24/10, Kalleberg, Kristopher kristopher.kalleb...@unilever.com
wrote:
From: Kalleberg, Kristopher
I always did HIER at pH6 for BCL-2, diluted at 1:10 (DAKO Ab) during 30 min
incubarion. FFPE tonsil as control.
René J.
--- On Wed, 2/24/10, Hannen, Valerie valerie.han...@parrishmed.com wrote:
From: Hannen, Valerie valerie.han...@parrishmed.com
Subject: [Histonet] Bcl-2
To:
I never used preservatives but I also never stored the buffer more than 5 days.
René J.
--- On Wed, 2/24/10, Amos Brooks amosbro...@gmail.com wrote:
From: Amos Brooks amosbro...@gmail.com
Subject: [Histonet] Tris Buffer Preservative
To: histonet@lists.utsouthwestern.edu
Is there a good Sirius Red procedure used to stain collagen
And where can I find the powder
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Thanks for everyone's help
From: John Kiernan [mailto:jkier...@uwo.ca]
Sent: Wednesday, February 24, 2010 11:36 AM
To: Nails, Felton
Cc: histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Sirius Red
You'll find brief instructions for the picro-sirius red
I use the Puchtler's Picro-Sirius Red Stain that I got from Stains
File online.
This stain works beautifully and the collagen is really pretty when
using polorized light microscopy.
The Sirius Red that I use was here in the lab so I didn't have to buy
it but it is Sirius Red F3B.
Andi
Kris,
Formalin pigment would give false positive staining with Fontana Masson.
Gudrun
-Ursprüngliche Nachricht-
Von: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] Im Auftrag von Cynthia
Pyse
Gesendet: Mittwoch, 24. Februar 2010 18:05
An:
Hi All,
Does anyone have any tips on reducing background staining when attempting to
detect mouse monoclonal antibodies on mouse tissue? We currently use Vector's
M.O.M kit - it works great on PPFE tissue with nice specific staining after
pepsin unmasking, but in frozen tissue the background
We have a long-handled scraper and use it periodically.
Jeanine Bartlett
Infectious Diseases Pathology Branch
(404) 639-3590
jeanine.bartl...@cdc.hhs.gov
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
We also use the long-handled scraper. Our greatest problem though, was the
hallway outside of Histology where non-technical staff would be walking in
heels. We eventually had that hall carpeted, which has been a great improvement.
-Original Message-
From:
We just bought everyone skates.
Seriously, we have a scraper that we use, along with the various mats. What we
just did was lay the traction strips on the floor outside of the Histology lab.
That was the area were most people, myself included have slipped and fallen.
Ironically, we found no
Hello, Amos,
It is pretty straightforward to make fresh, why would you want to
store it? We use sterile 1M Tris, pH 7.4, and 4M NaCl as stocks, they
are concentrated enough that nothing obvious grows in them, dilute
the volume you need, pH if needed, (add the Tween if needed), and
store in
Hi All,
I am trying to get AMPHYL disinfectant for the decon procedure for
ventana XT but heard that the product is discontnued by the manufacturers.
If anyone is using a substitute for this, please give me the vendor and
the part number.
Thanks
Nirmala Srishan
Holy Name Hospital is
Does anyone know of a reliable company to purchase FISH probes from (other
than Abbott)?
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
IDLabs http://www.idlabs.com/home/ works great for us.
Cambio is referenced a lot in the literature, but their Y-chromosome
porcine probes didn't work for us. http://www.cambio.co.uk/home
--On Wednesday, February 24, 2010 2:42 PM -0500 dcoj...@tampabay.rr.com
wrote:
Does anyone know of
What types of mouse tissue are you working with? Are they fresh frozen with
post-fixation or fixed frozen? Do you block biotin? Do you have an isotype
control and a no primary control? I am thinking biotin's the likely culprit as
the kit doesn't come with the very necessary biotin blocking
Not sure if you were asking me or not and it's a broad answer but VE-cadherin
is a good one - the best overall marker of endothelium. vWF is another one that
works well for most tumors. If staining mouse organs, if you let me know what
tissue you are staining I can recommend the best specific
Looking for part-time histotech Private lab in Plano Tx. 972 981 3108
The information contained in this message and any attachments is intended only
for the use of the individual or entity to which it is addressed, and may
contain information that is PRIVILEGED, CONFIDENTIAL, and exempt from
I was wondering how others are snap freezing tissue? We have been using
a histobath (a refrigerator device that cools isopentane for freezing
tissue), but it has died. I would love to have another Histobath, but
they are no longer carried by the vendor that I originally bought mine
from. Does
I have used the Gayle Callis method of freezing tissue for histological
applications for years with great success :) The tissues look fantastic.
Essentially float out a metal pan (like the ones you sterilize surgical tools
in) on a liquid nitrogen bath (in a styrofoam container or large
Contact Jim Mullen at Hacker Instruments (800) 442-2537. He has a demo
CliniRF that I'm sure you can get at a good price.
Dorothy
Dorothy Traczyk
MTA Histology LLC
In a message dated 2/24/2010 4:55:55 P.M. Eastern Standard Time,
laurie.colb...@huntingtonhospital.com writes:
I was
You made me worried there for a minute, Charles - I've spent a lot of time
cryosectioning rather than using PPFE! But luckily dehydrating,
rehydrating and post-fix seemed to completely get rid of the background I
was experiencing. No idea why it works, but it did. (We cryoprotect In
sucrose, then
Dear all,
I am going to decal and process PIG femur and lumbar vertebrates. I only have
experience on soft tissues. Anyone can suggest any protocols in
decalcification and processing? Many thanks in advance.
Cheers,
Victor
___
Histonet
I have noticed that most slips happen in the junctions between the
paraffin covered floors and uncoated floors, such as doorways to
outside halls. The change in traction does it. Also, hard soled shoes are
fine, as long as they have a build up of paraffin on them. If a visitor (or
30 matches
Mail list logo